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Post-traumatic; Arthrosis clinical trials

View clinical trials related to Post-traumatic; Arthrosis.

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NCT ID: NCT03226808 Active, not recruiting - Osteoarthritis Clinical Trials

Vivacit-E Post-market Follow-up Study

Start date: October 1, 2013
Phase: N/A
Study type: Interventional

The objectives of this study are to obtain clinical performance (outcomes) data and survivorship for commercially available Vivacit-E (HXPE) liners. This will be done by analysis of polyethylene wear, validated outcome measurement tools, radiographs, and reported adverse events data.

NCT ID: NCT03111407 Completed - Knee Osteoarthritis Clinical Trials

iAssist vs. Conventional Instrumentation in Total Knee Arthroplasty

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this prospective study is to evaluate Zimmer® iASSISTâ„¢ with respect to radiographic, clinical and economic outcomes and compared to conventional instrumentation in primary total knee arthroplasty (NexGen or Persona knee implants).

NCT ID: NCT02756702 Completed - Clinical trials for Rheumatoid Arthritis

All Polyethylene Tibia-VEGA Kiel

APT-VEGA_KI
Start date: March 2016
Phase:
Study type: Observational

Obligatory Post-Marketing Clinical Follow-up (PMCF) as part of the post marketing surveillance plan for the product under investigation For this PMCF only CE-marked medical devices will be used within their intended purpose and no additional invasive or other stressful examinations are to be carried out (acc. to MPG §23b).

NCT ID: NCT02679352 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

SMR Stemless Shoulder Arthroplasty Clinical Study

Start date: March 2016
Phase: N/A
Study type: Interventional

Shoulder arthroplasty is a reliable procedure for the treatment of severe shoulder joint diseases to relieve pain and restore shoulder function. Shoulder implants commonly used are characterised by a humeral stem and complications related to the stem are not infrequent. These include: bone stock loss, intraoperative and postoperative break around the implant, malpositioning of the humeral component and difficult eradication of infections inside the bone around the implant. With the aim of reducing stem-related complications, a novel prosthesis characterised by a stem-less design has been developed. The objective of this study is therefore to explore how well people recover after shoulder replacement with this novel stem-less shoulder prosthesis. This will be assessed over 5 years in three different countries in Europe using patient completed questionnaires and clinical and radiographic assessments.

NCT ID: NCT02503891 Recruiting - Clinical trials for Rheumatoid Arthritis

AL-2 MP-1 (Polyimide) Acetabular Liner

Start date: September 15, 2017
Phase: N/A
Study type: Interventional

M.M.A.TECH Ltd. product is an Acetabular Liner Family produced of an advanced polyimide - MP-1â„¢. M.M.A.TECH Ltd. produces the Liners according to EN ISO 13485:2012 approved manufacturing process and supplies them to the customer. The aim of this study is to evaluate, in the frame of PMCF, the safety and performance of using AL-X MP1 Polyimide Acetabular liners in Total Hip Replacement surgery by clinical following up of patients for a period of 2 years .

NCT ID: NCT02399046 Completed - Osteoarthritis Clinical Trials

A Clinical Trial Study of Knee System in Primary Total Knee Arthroplasty in China

Start date: August 17, 2017
Phase: N/A
Study type: Interventional

A clinical trial of total knee system used in Primary Total Knee Arthroplasty in China.

NCT ID: NCT01422564 Terminated - Clinical trials for Rheumatoid Arthritis

Metal on Metal Versus Metal on Highly Crossed Linked Polyethylene Sytem

MOM
Start date: January 2007
Phase: Phase 4
Study type: Interventional

This trial will evaluate the 36mm or greater metal head on metal hip system and compare it to the 32mm or 28mm metal head on polyethylene (liner) hip system in patients receiving a primary cementless total hip replacement.

NCT ID: NCT01413061 Completed - Clinical trials for Post-traumatic; Arthrosis

Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft

Start date: June 2010
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to evaluate the outcome of implanting AlloStem® graft with appropriate rigid internal fixation hardware as an alternative to autograft bone graft with rigid fixation in subtalar arthrodesis procedures. The primary objective of this clinical trial is to compare the overall fusion rate of the investigational to the control treatment. Fusion will be determined by clinical findings, radiographs and computed tomography (CT) of the subtalar joint 24 weeks (6 months) after the trial surgery.

NCT ID: NCT00822640 Completed - Clinical trials for Rheumatoid Arthritis

Comparison of Rotating vs. Fixed Platform of the COLUMBUS Knee Prosthesis

Start date: March 2004
Phase: Phase 4
Study type: Interventional

A population of 100 patients randomised to rotating and fixed PE inlays in the Columbus knee prosthesis received a navigated TKR. Knee Society Score as primary endpoint, Oxford Score, and postoperative ROM after one year will be compared.

NCT ID: NCT00492973 Completed - Osteoarthritis Clinical Trials

Do Corticosteroid Injections During Total Knee Replacement Improve Early Clinical Results?

Start date: March 2006
Phase: N/A
Study type: Interventional

Prior to surgery, a pharmacist will randomly assign participating patients to one of two groups. One group will get an injection in the knee during surgery that contains medications to limit pain and an antibiotic. A second group will get an injection in the knee during surgery that contains the same pain medications and antibiotic along with a corticosteroid to control inflammation. Corticosteroids are anti-inflammatory medications, not to be confused with muscle-building anabolic steroids you may have heard about in the news. Each patient will have an equal chance of being in either of the two groups. This study will test the safety and efficacy of methylprednisolone acetate in the treatment of pain and inflammation following total knee replacement.